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Quality Control Administrator (Medical)

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Staff Solutions
πŸ“ Cape Town, South Africa
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Location Cape Town
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Posted June 10, 2026
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Commute Local Area
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Job Description

Key Responsibilities
Regulatory Affairs


  • Ensure compliance with applicable medical device regulations (e.g., SAHPRA, FDA, EU MDR, ISO 13485, ISO 14971).

  • Prepare, submit, and maintain product registrations, licenses, and approvals with regulatory authorities.

  • Monitor regulatory changes and advise management on potential impact to business and products.

  • Support audits and inspections by regulatory authorities and notified bodies.

  • Maintain technical documentation, regulatory files, and product labeling compliance.


Compliance


  • Develop, implement, and monitor compliance programs in line with company policies, codes of conduct, and industry standards.

  • Conduct compliance risk assessments and recommend corrective actions.

  • Ensure adherence to anti-bribery, anti-corruption, data privacy, and ethical marketing practices....

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πŸ“ Location Details

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City
Cape Town
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Country
South Africa
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Commute
Local Area

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